FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

AltiVate Reverse® Glenoid

K Number: K252141 · Decision Aug 5, 2025
Classifications
1
FEI Numbers
191
Registration Numbers
191
Same Product Code
203
Applicant Total
81
Review Days
28

Basic Information

Device Name
AltiVate Reverse® Glenoid
K Number
K252141
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3660
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Encore Medical L.P.
Date Received
July 8, 2025
Decision Date
August 5, 2025
Product Code
PHX
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
PHX Shoulder Prosthesis, Reverse Configuration

Similar 510(k) Clearances

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Other Clearances by Encore Medical L.P.

K Number Device Name
K252567 AltiVate Reverse® ADLC Glenosphere
K252974 EMPOWR Knee
K251833 EMPOWR Acetabular® Liner Extension
K251776 EMPOWR Revision Knee™ (EMPOWR Revision VVC+, e+ Tibial Insert)
K251241 EMPOWR Revision Knee™ (EMPOWR Revision Knee™ Symmetric TT Cones)
K251184 AltiVate Reverse Shoulder System; RSP Shoulder System; SMR Shoulder System; PRIMA Humeral System; PRIMA Glenoid System
K241483 ceramys™ femoral head system
K233481 AltiVate Reverse® Glenoid
K222592 AltiVate® Anatomic Shoulder AG e+™ with Markers
K213387 AltiVate® Anatomic Shoulder AG e+™ with Markers
Search all 81 clearances from Encore Medical L.P. →